About Us
History
2024
2024.10
- Renewal of Medical Device Manufacturing and Quality Management Standards Certificate (GMP) KTC-ABBA-21568
- Supervised by MFDS and Korea Testing Certification Institute (KTC)
2024.09
- Submission of Designated Audit Application to Financial Supervisory Service External Audit Report System
2024.08
- Lead Underwriting Agreement for KOSDAQ Listing with Hana Securities, Convertible Bond Issuance (Pre-IPO Investment)
2024.06
- RCPS Issuance: 1,748,810 Preferred Shares at KRW 6,290 per share, Totaling KRW 11,000,014,900
2024.04
- SME Certification 0010-2024-317952, Supervised by the Ministry of SMEs and Startups
2024.03
- China Trademark Patent Registration for REVOSTEM (ไนๅๆ้ป) No. 74344887
- Morocco Product Certification for Hilthera 4.0: 50624/2023/4381-2024/DM/DPS/DMP/18
2023~2020
2023.12
- $3 Million Export Tower Award – Korea International Trade Association
- Gyeonggi Province Export Achievement Award – Certificate No. 15121, supervised by the Ministry of SMEs and Startups
- Domestic ReWave Trademark Patent Registration – No. 40-2121470-0000
2023.11
- Official Distributor Status Granted to Shanghai REV-MED Co., Ltd. (Legal Entity Status Acquired in China)
- Inno-Biz Certification (Technology-Innovative Small Business) – Certificate No. R170605-01132, supervised by the Ministry of SMEs and Startups
- Tricell PRP Morocco Product Certification – Certification No. 50624/2023/4381-2024/DM/DPS/DMP/18
- Main-Biz Certification (Management-Innovative Small Business) – Certificate No. 230601-03281, supervised by the Ministry of SMEs and Startups
2023.08
- Establishment of Shanghai REV-MED Co., Ltd.
2022.10
- Issuance of Convertible Bonds (Pre-IPO Investment Secured)
- Veterinary Medical Device Manufacturing License Acquired
- Korea MFDS Approval (Class III): TriCell PRP UNI
2021.07
- Korea MFDS Approval (Class III): Blood Processing Device (NovaStem BC)
- Korea MFDS Approval (Class III): Bone Marrow Processing Device (NovaStem BMAC)
2020.11
- Inno-Biz Certification (Technology-Innovative Small Business)
- Korea MFDS Approval (Class III): Fat Separation Device (DUOCELL SVF KIT)
2020.04
- ISO 13485: 2018 Certification Acquired
- Hilthera 4.0 CE Certification Acquired
History
2024~
Renewal of Medical Device Manufacturing and Quality Management Standards Certificate (GMP) KTC-ABBA-21568
Supervised by MFDS and Korea Testing Certification Institute (KTC)
Submission of Designated Audit Application to Financial Supervisory Service External Audit Report System
Lead Underwriting Agreement for KOSDAQ Listing with Hana Securities, Convertible Bond Issuance (Pre-IPO Investment)
RCPS Issuance: 1,748,810 Preferred Shares at KRW 6,290 per share, Totaling KRW 11,000,014,900
SME Certification 0010-2024-317952, Supervised by the Ministry of SMEs and Startups
China Trademark Patent Registration for REVOSTEM (ไนๅๆ้ป) No. 74344887
Morocco Product Certification for Hilthera 4.0: 50624/2023/4381-2024/DM/DPS/DMP/18
2019~2017
2019.01
- Taiwan Medical Device Certification: Hilthera 4.0
2018.12
- Development and Commercialization of Bone Marrow Processing Device
2018.11
- World-Class Product Certification
2018.09
- Development of Large-Capacity 50ml Autologous Bone Marrow Processing Device
2018.03
- Opening of REV-MED Stem Cell Research Institute
2017.05
- Opening of Laser Division
2017.03
- Japan PMDA Approval: Blood Processing Device (Class III, TriCell PRP)
2016~2009
2016.08
- Health Technology (NET) Certification
2016.06
- China CFDA (NMPA) Approval: Blood Processing Device (Class III, TriCell PRP)
2016.03
- Korean MFDS Approval: Bone Marrow Processing Device (Class III, TriCell BMC)
2015.12
- Establishment of REV-MED International GmbH in Germany (Joint Venture)
2015.01~2015.12
- Blood Processing Device Development (Gyeonggi Science and Technology Promotion Agency)
2014.07~2015.07
- Development of Autologous Bone Marrow-Derived Stem Cell and Nucleated Cell Concentration Kit
2013.10
- Opening of Corporate Research Institute
2012.10
- ISO 13485: 2012 Certification Acquired
- TriCell PRP CE Certification Acquired
2012.07
- Korean MFDS Approval: Blood Processing Device (Class III, TriCell PRP)
2009.01
- Establishment of REV-MED Corporation
2023~2020
$3 Million Export Tower Award – Korea International Trade Association
Gyeonggi Province Export Achievement Award – Certificate No. 15121, supervised by the Ministry of SMEs and Startups
Domestic ReWave Trademark Patent Registration – No. 40-2121470-0000
Official Distributor Status Granted to Shanghai REV-MED Co., Ltd. (Legal Entity Status Acquired in China)
Inno-Biz Certification (Technology-Innovative Small Business) – Certificate No. R170605-01132, supervised by the Ministry of SMEs and Startups
Tricell PRP Morocco Product Certification – Certification No. 50624/2023/4381-2024/DM/DPS/DMP/18
Main-Biz Certification (Management-Innovative Small Business) – Certificate No. 230601-03281, supervised by the Ministry of SMEs and Startups
Establishment of Shanghai REV-MED Co., Ltd.
Issuance of Convertible Bonds (Pre-IPO Investment Secured)
Veterinary Medical Device Manufacturing License Acquired
Korea MFDS Approval (Class III): TriCell PRP UNI
Korea MFDS Approval (Class III): Blood Processing Device (NovaStem BC)
Korea MFDS Approval (Class III): Bone Marrow Processing Device (NovaStem BMAC)
Inno-Biz Certification (Technology-Innovative Small Business)
Korea MFDS Approval (Class III): Fat Separation Device (DUOCELL SVF KIT)
ISO 13485: 2018 Certification Acquired
Hilthera 4.0 CE Certification Acquired
2019~2017
Taiwan Medical Device Certification: Hilthera 4.0
Development and Commercialization of Bone Marrow Processing Device
World-Class Product Certification
Development of Large-Capacity 50ml Autologous Bone Marrow Processing Device
Opening of REV-MED Stem Cell Research Institute
Opening of Laser Division
Japan PMDA Approval: Blood Processing Device (Class III, TriCell PRP)
2016~2009
Health Technology (NET) Certification
China CFDA (NMPA) Approval: Blood Processing Device (Class III, TriCell PRP)
Korean MFDS Approval: Bone Marrow Processing Device (Class III, TriCell BMC)
Establishment of REV-MED International GmbH in Germany (Joint Venture)
Blood Processing Device Development (Gyeonggi Science and Technology Promotion Agency)
Development of Autologous Bone Marrow-Derived Stem Cell and Nucleated Cell Concentration Kit
Opening of Corporate Research Institute
ISO 13485: 2012 Certification Acquired
TriCell PRP CE Certification Acquired
Korean MFDS Approval: Blood Processing Device (Class III, TriCell PRP)
Establishment of REV-MED Corporation